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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1915972생성일: 2026년 10월 26일

Diethylamine → 9H-fluoren-9-ylmethyl N-ethylcarbamate;methyl 2-[[1-[[(2S)-2-formamido-3-tritylsulfanylpropanoyl]amino]cyclopropanecarbonyl]amino]acetate

https://huagongshe.com/reaction/1915972

반응식

참여 물질

역할이름HCID투입량
반응물DiethylamineHCID 8021—
반응물DiisopropylethylamineHCID 81531—
반응물Fmoc-Gly-OHHCID 93124—
반응물PyBOPHCID 2724699—
반응물{(R)-2-[(S)-2-(9H-Fluoren-9-ylmethoxycarbonylamino)-3-tritylsulfanyl-propionylamino]-3-methyl-butyrylamino}-acetic acid methyl esterHCID 57696983—
용매AcetonitrileHCID 6342—
용매DichloromethaneHCID 6344—
용매Acetonitrile methylene chlorideHCID 21877088—
생성물9H-fluoren-9-ylmethyl N-ethylcarbamate;methyl 2-[[1-[[(2S)-2-formamido-3-tritylsulfanylpropanoyl]amino]cyclopropanecarbonyl]amino]acetateHCID 86653402137.6%

반응 단계

To a solution of 1 (310.5 mg, 0.420 mmol) in MeCN/CH2Cl2 (10 mL/19 mL) under Ar(g) was added diethylamine (2.9 mL, 10% v/v) and the reaction mixture stirred at rt for 1 h 50 min. The solvent was removed in vacuo, the crude mixture treated with MeCN (3×20 mL) and the solvent was removed under reduced pressure. The crude amine was then dried under high vacuum for 1 h. Then to a solution of PyBOP (234.9 mg, 0.451 mmol) and FmocGly-OH (133.86 mg, 0.450 mmol) in CH2Cl2 (20 mL) was added diisopropylethylamine (0.25 mL, 1.44 mmol) under Ar(g) with stirring for 3 min. A solution of the resultant deprotected amine of 1 in MeCN (20 mL) was added, and the resulting mixture was allowed to stir at rt for 16 h. The solvent was then removed in vacuo. Purification by flash column chromatography on silica (eluant 1:99-3:97-5:95 MeOH/CH2Cl2) gave a white solid. The material was washed with 1M HCl (aq), dried (MgSO4) and concentrated in vacuo to give 2 (228.6 mg, 0.289 mmol, 68%) as a white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08614193B2
출처 데이터셋uspto-grants-2013_12
ORD IDord-48eb9fbe6dff47f5bc5c0937581b752b
출처 메모uspto-grants-2013_12